5-Methyl-4-nitrothiophene-2-carboxamide

95%

Reagent Code: #203442
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CAS Number 36050-10-9

science Other reagents with same CAS 36050-10-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 186.19 g/mol
Formula C₆H₆N₂O₃S
badge Registry Numbers
MDL Number MFCD01025640
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, light-proof

description Product Description

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its structure allows for functionalization at multiple sites, making it valuable in creating active ingredients with enhanced selectivity and efficacy. It is also employed in research for novel heterocyclic compounds targeting crop protection agents. The presence of both electron-withdrawing and electron-donating groups facilitates coupling reactions and heterocycle formation in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,530.00
inventory 1g
10-20 days ฿39,100.00
inventory 250mg
10-20 days ฿14,490.00

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5-Methyl-4-nitrothiophene-2-carboxamide
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Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its structure allows for functionalization at multiple sites, making it valuable in creating active ingredients with enhanced selectivity and efficacy. It is also employed in research for novel heterocyclic compounds targeting crop protection agents. The presence of both electron-withdrawing and electron-donating groups facilitates coupling reactions and heterocy

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its structure allows for functionalization at multiple sites, making it valuable in creating active ingredients with enhanced selectivity and efficacy. It is also employed in research for novel heterocyclic compounds targeting crop protection agents. The presence of both electron-withdrawing and electron-donating groups facilitates coupling reactions and heterocycle formation in medicinal chemistry.

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